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MOCRA Compliance for Businesses

Posted on December 31, 2024

The Introduction to MOCRA Requirements

The Modernization of Cosmetics Regulation Act (MOCRA) is a significant regulatory framework established by the U.S. Food and Drug Administration (FDA). This law, which was passed in 2022, addresses a gap in the regulation of cosmetics in the United States. MOCRA mandates that all businesses in the cosmetic industry, from manufacturers to retailers, comply with specific guidelines to ensure the safety, labeling, and transparency of cosmetic products. One of the key aspects of MOCRA is its requirement for cosmetic manufacturers to register their facilities with the FDA. This registration process aims to enhance oversight and traceability within the industry, ensuring that products are safe for consumers.

The Key Compliance Aspects for Businesses

MOCRA establishes several essential compliance aspects that businesses must adhere to in order to meet FDA standards. These include maintaining records of product formulations and ingredients, ensuring that products do not contain harmful substances, and updating product labels with clear and accurate information. Companies must also notify the FDA about any cosmetic products that are intended to be marketed in the United States. This registration and notification process allows the FDA to monitor new and existing products, ensuring that any potential risks are identified early. Businesses also need to ensure that their products are not misbranded or adulterated, as defined under the act.

The Reporting and Record-Keeping Requirements

In addition to product registration and labeling requirements, MOCRA imposes rigorous reporting and record-keeping obligations on businesses. Manufacturers are required to maintain detailed records about the safety of their products, including data on ingredient safety and testing. These records must be readily accessible for FDA inspection. Companies must also notify the FDA of any adverse reactions or complaints related to their products. The act empowers the FDA to request access to these records to investigate potential violations or safety concerns. Therefore, businesses must have robust systems in place to comply with MOCRA’s reporting requirements to avoid penalties or legal challenges. mocra requirements

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